Calves symptoms and conditions

okinawak so sorry to hear about your daughter. All I can relate to you guys is my personal experience. I was on Norimin for a couple of years from the age of 19. For the last year (up until a couple of months ago) I was on Yasmin. I experienced anxiety whilst taking these pills which I attributed to stress, but since I have been off the pills I am feeling fantastic. I stopped taking Yasmin because I was experiencing other things like pains in my calves, hair loss and getting spider veins, loss of libido (I'm only 23). :-( I decided upon reading other experiences on this page to stop taking Yasmin. I am happy to report back that I am feeling great... Fantastic in fact. I won't say that its directly related to yasmin as I have no way of proving that. All I can say is how I felt during and after. And for the last three months I have felt greater confidence in my ability to deal with what life throws at me. I am feeling happier all the time, and I think my libido is improving. All the best to you guys, and all those out there worried about symptoms, please go see your doctor!

Yaz increases your potassium levels, SO DO NOT eat anything with Potassium or take any medications that will increase your potassium. You will over load your system and make it even worse on you. You really need to read the enclosed brouchure that came with Yaz from front to back to ensure you are fully aware of what you are taking and all the risks and side effects you will get. I had the same issues with my calves and it was not normal at all. Since I have stopped taking Yaz all my symtoms are gone and physically I feel normal again. I have not gotten my period yet, which I thought would come when I stopped taking Yaz, but nothing yet. I experienced anxiety attacks whenever I tried to climax so I understand what you are talking about. Yaz lowers your testosterone levels which drives your sex lfe, so there may be no hope for it to be normal again as long as you are on Yaz.

Hi all! I'm 22 and will be starting on my 3rd Yaz cycle...I have noticed a few things about this drug...My PMDD symptoms have seemed to decline quite a bit-although i still get very emotional. My acne has slightly cleared up and my periods last 4 days the most with minimal cramps. I have been experiencing muscle spasms in my calves but this may also be from not having enough potassium in my diet. My biggest concern however, would be the decrease in my sex drive...Yaz was the last thing my boyfriend and i thought it could be but the more we read about it, the more we are convinced. I literally went from having sex a few times a day to not wanting to be bothered with it. this is lame, i'm young and enjoy being fun and playful and spontaneous with my boyfriend but no matter how hard we try, I can't reach climax (something that was never a problem before). since this is the only oral contraceptive I have tried that hasn't given me nausea or headaches, i am hoping this libido change will go back to normal. if it doesn't by the end of this cycle i will have to try something else. any ideas?

Update on my post of Aug. 11th. I did see a neurologist who was a bit skeptical, but after looking it up did acknowledge that this drug can cause tendon ruptures, etc. Later that week he did a nerve conduction study, both the one with the needles and the one where they shock the muscles. He was happy to report that I did not have any "nerve" damage. I had already told him that I did not think I had neuropathy as the numbness had gone away and was just replaced by the constant pain in my joints, etc. I then went to see my rheumatologist who was also just as skeptical that the drug could be causing all the pain I was describing. She said she had had three patients with tendon ruptures, but nothing else. I really don't care what she believes, and I told her so. I know what happened and what horrible pain I have been in ever since. I hate to report that the pain in my feet, knees, hands, hips, back and now my neck are not any better. My insomnia is some better, but I am taking more Lyrica. I tried a different antibiotic yesterday for the sinus infection called Clindamycin. OMG! I took one pill and within a few minutes had unbelievable heartburn. That lasted for 12 hours, along with reflux, burping, weird stomach noises. Now, I can't take that. Doctor called in a prescription for Augmentin this morning. Afraid to try anything now, but guess I will give it a shot. Is anyone getting any better from their joint or muscle pain? Some encourgement would be good. Thanks.

I've been taking Levaquin for about 3 weeks. Last week, suddenly, every joint in my body started aching. I mean from my neck, hands, hips, knees, ankles, feet, everything. For the past week, when I wake up, I can't even make a fist without experiencing excruciating pain. I've always been very active, running, basketball, soccer, skiing, you name it, so this is scaring the heck out of me. I'm 47 years old, and up until a week ago, I was hiking with my family, running everyday with my dog. Now I feel like I'm 100 years old. It hurts to walk, stand up, etc! I have an appointment with my doctor tomorrow! I'm ticked about this!

Well...i'm only 17 years old and i have been trying EVERYTHING to get rid of my 2 week long heavy period and extremely severe cramping. I have been on 3 different kinds of oral BC and i would still bleed for 2 weeks. So i tried the Mirena IUD and that was the worst idea of my life. It went in fine but about 10 minutes later i was in a extreme amount of pain (and i have a very high pain tolerance, broke 3 ribs and didn't cry) i called my gyno back and he prescribed me a pain medication but it didn't work. After trying 3 different pain medications and an antibiotic i had enough. I went to the hospital and was prescribed percocet and that helped. I went back a few days later and had it taken out so now i am trying the NuvaRing. I put it in and a few hours later started cramping and having back pain. The next morning i had very bad nausea and cramping. Its about a week later now and i am experiencing headaches, nausea, quite bad cramping, bloating, tiredness all the time and i just don't feel myself anymore. I am calling my gyno back to see what he suggests but i'm looking for any ideas or suggestions until i get a hold of him. Thanks

I was prescribed 500 mg Levaquin for 5 days for a uti.

After two days I got a cramp in my left calf muscle.

It's been 2 weeks now. My UTI still remains and I feel horrible. I'm taking Vicodin for all over pain. My calves, lower back, shoulders and knees ache badly. I feel like I have the flu, but without the nausea.

My Doc prescribed Nitrofurantoin to treat the UTI again. Can't wait to check it out.

I just found this site and have been reading the posts and I'm so pissed.

I read some posts that said this poison had left a metal taste in some mouths, so tomorrow I'm going to a CHELATION treatment center and start IV treatments. Chelation by intraveneous is good for getting metals out of your system. I had some treatments about 10 years ago to clean out my arteries and felt better, so hopefully this will work. I'll post the results here.

Was on Vytorin for 2 years & experienced no noticeable side effects during that time. It lowered my cholesterol to 179. Had a hysterectomy (complete) in Dec., 2007. In May, 2008, I began a sudden on-set of severe numbness in both hands (especially when lying down)--classic carpal tunnel symptoms and intense pain in all joints. When I move from a sitting position to stand up, I can hardly do it. This is what I thought I would feel like at maybe 80 years old--not 46 yrs. I thought maybe it was because I'm not taking hormone replacements, but my doctor said it could be the Vytorin & he took me off of it. I've been off for 2 months, but the symptoms are not improving. The carpal tunnel seems to have lightened up a bit, but the joint pain (especially hips) has not gotten any better. I wonder if it ever will????? Also experience fatigue, foot pain, & weak fingers.

I started taking Yaz 1.5 months ago. During the first pack I saw little to no side effects, period lasted 4 days and was drastically lighter than before starting Yaz. Before Yaz I would bleed for 5 days and go thru a bag of super pads, with Yaz I barely bleed enough to use 6 pads in 4 days, BIG difference!

Now into the second pack I had a headache for 3 days straight, I am having stomach pain, I eat only because I know I have to or I wouldn't eat at all, I have no sex drive even though I think about sex and things excite me I just don't want to be bothered with the physical act, my breast are tender all the time, my lower back is in pain, charlie-horses in my calves and back of thighs, I am constipated, and very gassie!

Took first pill (5mg) on 7/8. Second on 7/9. After lunch on 7/9, food stayed in stomach and would not digest. Felt like a huge lump. Digestion continues to be a problem. No appetite. Food does not look good. On 7/11, developed two hives with large red areas surrounding them, however, they were not itchy. Became quite tired also. Allergy symptoms of itching eyes, watering eyes, itching throat, stuffiness developed. Headaches to the point of taking a pain reliever. Developed muscle cramping in calves on 7/15. Still great difficulty eating with no appetite. Existing hiatal hernia became a problem at night with nausea. Terrible flatulence also. Exhaustion is now the description, not just tired. Feeling depressed, but perhaps that is a result of the exhaustion. Blood in urine on 7/18, the final straw. Discontinued med on 7/18. Hives have still not cleared up totally (7/28) and the tiredness has still not gone away. I have been told that when you have hives on the outside, you have hives on the inside too. I would never take this med again. Going to look into biofeedback.

Took first pill (5mg) on 7/8. Second on 7/9. After lunch on 7/9, food stayed in stomach and would not digest. Felt like a huge lump. Digestion continues to be a problem. On 7/11, developed two hives with large red areas surrounding them, however, they were not itchy. Became quite tired also. Allergy symptoms of itching eyes, watering eyes, itching throat, stuffiness developed. Developed muscle cramping in calves on 7/15. Still great difficulty eating with no appetite. Existing hiatal hernia became a problem at night. Terrible flatulence also. Exhaustion is now the description, not tired. Feeling depressed, but perhaps that is a result of the exhaustion. Discontinued med on 7/18. Hives have still not cleared up totally (7/28) and the tiredness has still not gone away. I have been told that when you have hives on the outside, you have hives on the inside too. I would never take this med.

I'm 22 years old and I have been on Yasmin for 3 years. The first year it was fine, but the next year I began getting panic attacks which I never even believed in until I had one myself. I've had severe anxiety that is uncontrollable and doesn't allow me to sleep at night. Let's not even talk about the emotional mood swings during my period. My boyfriend knows when it's that time of the month because I'm not myself. I will cry over things that would never make me cry in a million years. I'm mean and moody and then 20 minutes later I feel bad, but then I'm crabby again. Weight gain has not been a problem for me only about 3-5 pounds, but my breasts did go from a large B to a D. My boobs definitely do not fit my body. I have noticed a lot of hair fall but I just thought it was normal. I too have had problems with my potassium levels as I would get leg cramps in the middle of the night so I began drinking Gatorade and eating bananas every morning which has helped. I love being on birth control because it helps me plan accordingly, but I just don't feel like myself anymore. I am always hungry and am never full. I literally have to tell myself out loud that I'm done eating because it doesn't trigger for me. I have had a stomach ache nearly everyday of being on the pill. I became addicted to TUMS which only made it worse. I thought it was stress related which it might be, but I literally do not go to the bathroom for 4 or 5 days and it is soooo painful. Another thing is that I have no sex drive. I really have to prepare myself for it otherwise sex does not even occur to me. My boyfriend thinks I'm not attracted to him, but I AM! We just moved in together and you would think it was "freedom" but I'm just motivated to have sex. This is not normal for a 22 year old healthy female with an extremely hot man.

Anyway, I just went to the doctor and told her I was interested in Yaz. She gave me a few sample packs which I will begin next week. I'm hoping for the best and I truly do believe that birth control is a trial and error process. Everyone's bodies are different and you need to find the one that works best for you! I will write again once I know how Yaz works out.

-MCL

Took the perscription (500 mg, 2X daily) for three days before I started having bad side effects, then it hit me like a ton of bricks, and I quit immediately. My digestion has been real messed up, my stomach and intestines have felt as though they had a meat grinder turned on inside. My head has felt as though the top of it was going to come off. I've been off the pills for 3 days now and my head is beginning to feel better. My major complaint now is that my legs ache. My thighs mostly, but also my calves some. I had no idea I would get so sick from an antibiotic.

I have been feeling a sensation of pins and needles in my calves and a feeling of numbness in my feet. I know this is listed as a potential side effect but what are the indications? Also, dizziness and tiredness. I have been on Singulair for about 9 months.

I am so relieved to have found this site. I suffer from PCOS (Polycycstic Ovarian Syndrome). I am also morbidly obese, but I have been on a diet for 3 years and I enjoy the diet, sounds funny, but it is true. I lost 30 pounds the first year. Now, I have gained it all back, I can't do anything, I am in so much pain. I have back pain, knee pain, I have swelling in my legs they are so huge (the calves) They have grown three inches in circumference since I started the progesterone therapies. I have pitting edema in both my legs and my hands swell all the time. The only way to reduce the swelling in my hands is to hold my arms over my head for about 15 minutes and that seems to help enough to get my rings off. Mirena was supposed to NOT cause any side effects. Well let me tell you I got them all. The same way I did with the pill form. Only Mirena took longer to enter into my system. I am waiting for my Doctor to get back from vacation and I will be insisting on its removal.

Here is my list:

Pitting Edema in arms and legs
Headaches
Severe abdominal pain
Severe backache
Heart palpitations
Constipation
Lack of appetite
SEVERE WEIGHT GAIN (how can this be, I have been a diet for three years...and I am sticking to it) MY PANTS won't fit anymore.
NO energy
Fatigue
Nightmares
Nausea
Dizziness
Unable to concentrate
Slight double vision (right eye only)
Anger
PIMPLES ( I am 38 for Pete's sake, I didn't have pimples as a teen!)

My Doctor lied. Plain and simple. He told me there would be no systemic side effects. Either Bayer (Mirena) is lying to him, or he is lying to me....either way...I see a class action lawsuit coming if they don't remove this thing. I will kill me if it stays in any longer. I just know it! For those it works for good. I am pleased. For those of us who is don't, I truly feel your pain!

I am so relieved to have found this site. I suffer from PCOS (Polycycstic Ovarian Syndrome). I am also morbidly obeses, but I have been on a diet for 3 years and I enjoy the diet, sounds funny, but it is true. I lost 30 pounds the first year. Now, I have gained it all back, I can't do anything, I am in so much pain. I have back pain, knee pain, I have swelling in my legs they are so huge (the calves) They have grown three inches in circumference since I started the progesterone therapies. I have pitting edema in both my legs and my hands swell all the time. The only way to reduce the swelling in my hands is to hold my arms over my head for about 15 minutes and that seems to help enough to get my rings off. Mirena was supposed to NOT cause any side effects. Well let me tell you I got them all. The same way I did with the pill form. Only Mirena took longer to enter into my system. I am waiting for my Doctor to get back from vacation and I will be insisting on its removal.

Here is my list:

Pitting Edema in arms and legs
Headaches
Severe abdominal pain
Severe backache
Heart palpitations
Constipation
Lack of appetite
SEVERE WEIGHT GAIN (how can this be, I have been a diet for three years...and I am sticking to it) MY PANTS won't fit anymore.
NO energy
Fatigue
Nightmares
Nausea
Dizziness
Unable to concentrate
Slight double vision (right eye only)
Anger

My Doctor lied. Plain and simple. He told me there would be no systemic side effects. Either Bayer (Mirena) is lying to him, or he is lying to me....either way...I see a class action lawsuit coming if they don't remove this thing. I will kill me if it stays in any longer. I just know it! For those it works for good. I am pleased. For those of us who is don't, I truly feel your pain!

Here is my Mirena Story.

I was 6 weeks post partum....I had mirena inserted...it was very painful and I was not warned about that.
About a week later I noticed yellowing in the whites of my eyes which I thought could be coming from a iron def. since I just gave birth. So I made sure I was eating well and taking vitamins. I also had severe itching at night especially on my ankles and legs. Oh and sex drive was gone. It was fine the 6 weeks after birth but as soon as mirena was in it was gone!!! I went to the doctor about a month after insertion and asked to have it removed, of course my doc said it couldn't be iud causing my problems...come back in a month...So I did....within this month I started having severe anxiety, insomnia and panic attacks, to the point were I actually thought I was loosing my mind. Of course again the doc told me that it wasn't iud and prescribed me an antidepressant which I reluctantly excepted. I'm not depressed...my life was perfect before mirena!!! I finally went back for the third time and decided I wasn't leaving until somebody took this thing out of me!

Here is a list of other side effects that I had/still have!!

acne
migraines
extreme lower back pain
numbness and tingling in hands and feet
vision problems
fogginess
An ADHD type feeling
inability to focus or concentrate
extreme fatigue
feeling of throat closing up
heart racing and palpitations
night sweats
sinusitus
dizziness and light headiness
headache

The problem here is that the doctors don't even know how extreme these side effects can be and they keep telling us that it's not the mirena. PLEASE trust your instinct.....I wanted to trust my doctor but I knew in my heart what was causing my problems...I am only 1 week post mirena and I am still having a lot of my problems but I can tell a difference. DON'T LET IT GET OUT OF HAND....TAKE IT OUT!!!!

DON'T GET MIRENA...IT MAY WORK WELL FOR SOME...BUT IN MY OPINION IT IS NOT WORTH THE CHANCE THAT THESE HORRIBLE SIDE EFFECTS COULD HAPPEN.....HAD I BEEN INFORMED PROPERLY I WOULD HAVE NEVER HAD MIRENA INSERTED!!

Good Luck Ladies!!

I was on Vytorin for about 3 years. Originally I was prescribed 40 mg and when my ldl didnt go down enough for the doctor. I was prescribed 80 mg a day about a year and a half ago. A bit of history....I had a heart attack at 33 years of age and at that time was given angioplasty. I am now 44 years old and have not had another attack. I have been having muscle pain for over year, although it feels more like my syatic sp? nerves in my lower back. My knees are so bad that I have been having to wear knee braces periodically and can no longer kneel without falling over in extreme pain. My muscles in my thighs have been deteriorating even though I have been working out with a personal trainer for over a year and my calves were getting huge to compensate. I also went to an eye dr. as I was having trouble reading and driving at night due to blurry vision. They said that I still had 20/20 vision and to start using very light reading glasses when reading and that should help. The last straw was when I was on vacation and had a terrible bout of paranoia. It was so bad that I can't even tell anyone what it was about. Another major effect that I have had over the years from any statin is the fact that my sexual urges are basically non existent.

Now for the good news!!!! In late April, after returning from my vacation, I decided that I wanted to see if the Vytorin/Simvastatin was giving me a majority of these symptoms and decided to quit cold turkey. Well 2 months later I can say that I feel about 90% better. I haven't had to use the reading glasses within 48 hours of stopping (I'm not even sure where they're at now). Within a week I noticed my libido returning and the paranoia completely gone. Within the last 2 weeks I have noticed my thigh muscles coming back and the muscles around my knees getting stronger. I am so thankful that I am returning back to normal!!

I will never, ever take another Statin again!!!!

Dry gagging cough, weight gain, charley horse in calves, but worse of all when I use the bathroom I have a terrible burning sensation in personal area of my body. Am using baby wipes instead of TP. The burning subsides for a while but of course is back when I have to use bathroom again. I think the diuretic in this pill may have some bearing on this symptom. I was checked for a bladder infection and it was negative, although a minute amount of red blood cells were found in my urine. I too, have had the very low BP readings, 90/68, etc. The first time this happened it frightened me so bad I got up and ran around our house and took BP again and it had risen within the normal range. I was on Hyzaar and my present doctor could not understand why I was on such a strong BP med. So he changed my to Lisinoprol HCTZ. Anyone having the same effect?

My doctor prescribed me this medication (3 days/2x a day) to treat a minor UTI. It did its job but now i have a horribly itchy rash on my feet and lower calves. Furthermore, I was already struggling with an eating disorder before I started this medication, and now it is way worse. It completely took away any appetite i had before

I have had so many shots of
Corticosteroids/NSAIDS/Steroids:

Triamcinolone Acetonide, Kenalog, Depo-Mardol, Lidocaine, Marvaine, Toradol, Epinephrine, Bextra, Xylocaine, Isovue.......on and on and now I do not walk hardly anymore.

I am married, no sex whatsoever! I stayed away from my husband for 3 years almost, living at my apartment. I just moved out by Eviction March 2, 2008. I did not pay rent for one year. I applied for disability since 1995. Won ALJ decision September 2006. I appealed the case being opened back to 1995. I wanted it go go back futher. Just appealed it again in 2008.

Okay, I am a simpleton out here needing a HERO to Take A Stand and Advocate for me.

I do not live with my husband. I live at his mother's home so that he comes and takes cares of us at the same time. She is 90 now. Can you imagine this? I have been reduced to a cripple.

I am a prisoner laid to rest by the BIG DRUG COMPANIES MISLEADING ME, IN NOT KNOWING ABOUT THE DISEASES THAT WOULD ATTACK ME IN THE ONLY LIFE THAT I HAVE.

I wonder if my hip bones have collasped. I have terrible bone pain.

I waddle like a duck, side to side with extreme pain until I freeze up and fall, but mostly, I live with a cane at my side when going out and about.

I now need a wheelchair.

From 1980's, 1990's and now all the way to 2008. I have all medicals.

It was not until 2003-2004 that my life took a turn for the worse.

Hips pain, arms pain, shoulders pain, pain in the Thorasic area to the tail bone area, right groin pain/pubic area pain/gentials, stomach sores/cut out, pain on the scalp, calves feel hard in side/stiff at all times, hamstrings are short,open sores have been on my face, arms and neck lasting for 4-6 mths, low back pain....all of me has been injected with the above crap.

I was doing quite well in life until 2004 when this Orthopedic doctor had shot my left shoulder 3 times.

After this June 2004 event above, and by September 2004 I had walking problems, blamed only on Fibromyalgia, DX 1989.

They took one blood test for Polyrheumatica.

I was fed 20 something meds in 2004.

By 2005 I was devestated in life, health and even wanting to be alive. For one full year I lived on the pot, using Lidocaine up the butt 3-4 times a day for the pain.

Now, looking back at this part, no wonder I had extreme skin blisters, hives, rashes, extreme sweating....this Lidocaine for rectum pain was harming me and no one took me off of it. I finally had my pharmacy tell me this was so wrong to be using 134.00 a month for over one year for pain. I stopped!!!! he seemed to say that I was being harmed.

Suddenly, at my clinic, all of my primary doctors began to do trigger point injections weekly, monthly and for 4 years for my Fibromyalgia comlaint. DX in 1989.

Many NSAIDS for one year, 2003-2004.

In 2003 I had a new denture and a few teeth extracted so that I smiled great when got married April 2003.

By August 2003 I was off the State HMO, had housing city of salem voucher for 5 years at my apartment and was planning to move out and be at my husband's home, but...by September 2003 I was already in some medical exams, new meds and was being normal to a point.

By late 2003 to mid-2004 I was feeling strange about my health. I felt as if I was being sucked dry of any fluids, weird to say, but it felt as if...hard to explain.

I was dizzy, vertigo, some balance problems and like itching, sweating and extreme fatigue. I felt like i was melting. My muscles felt like jello. I had no ability to stay upward on my spine.

I did complain to my dentist and doctors that I was feeling numb on my face and gums by may 2003.

After 2 years, leaving room for a possible lawsuit on the dentist/OS, I filed, had one deposition and my lawyer walked.

I had laughing gas for teeth extractions/numbing shots.

I thought that GAS/SHOTS was to be blamed, maybe the tools they used, or the water and I worked this case to the bitter end, sad to say, that a Lawyer Walked On Me.

By 2004 I did not know what hit me with my health issues..dentists/new meds/new marriage/new doctors involved.

I was in a drug stupor, taking almost 30 drugs from this clinic in 2004.

Prescribed and the samples of Vioxx, Mobic, Celebrex and Bextra.

I had so many Toradol shots to my spine and hips at this clinic and thought they had crippled me.

This doctor humiliated me.

Told me that I was a nut.

I now needed long term counseling with all of the body ailments they all told me. My primary doctor told me many times that NONE OF THE SPECIALIST NEEDED OR WANTED TO SEE ME FOR ANYTHING.

Nothing was hardly affecting me when I got married April 2003. I was a knock out!

The Gastro doctor had me on his 3 drugs also, including that daily Lidocaine up my butt. He did the endoscopy and colonscopy, bloodwork and he said I had Atrophic Mucosa.

He was in direct conflict with my Neurologist who did his own work and he claimed that I was Gluten sensitive, a Celiac now. He gave B12 shots and Folic Acid on top of all the other crap that I was taking.

The Hospital did a spinal tap and may tests.

The pain specialist did his epidurals 2 times.

I have had every NSAID they prescribed me.

I had sleeping pills.

I had anti-depressants.

I had Vicodin to Percacets and then they tried to get me on Methadone. One week on that crap was all.

I notice that Depo-Medrol, Marcaine, Lidocaine was mostly used thru out my life.

The pain specialist above that I used in 2006, also shot me with the epidurals 2 times before 2006, and the O.H.S.U. also shot me with all the above when they DX me with Fibromyalgia 1989.

Then many Toradol and Kenalog shots.

I live with daily diarrhea since 2005-2008.

My legs are always red every day with any walking, sleeping, sitting, balance is off, waddling gait.

My feet pain is as if I walk on glass or rocks....sharp pain now for 4 months.

Arachnoiditis fits me well. I have spoken with the doctor/expert that can test me.

I have been searching since early 2004.

I have no way to know who or what to blame.

I even thought that the MRI's Contrast Agents harmed me starting from the past to now.

I left the clinic that stole my life from me and now have a new doctor at Kaiser Permanente.

I am scared of all doctors now.

I have 4-5 meds right now.

Not one doctor or specialist will DX me. I have a thought below...

I fought the medical community WORLD WIDE back in 2002-2003 with the President Dr. Richard Willner, of Retired Association of Physcians and Surgeons. My two other sisters were in this heated debate.

I was told to expect danger at any time after this online 30 page cruel attack by the doctors on my wrongful death of my mother by her doctors/nursing home/hospital.

I proved this case.

The lawyer in Portland, Or. Judy Snyder told me I did extremely well proving this death was murder...but the Medical Consultant who did the summary of this death was hushed up!!! Later on, after another summary by Medical Consultant, she told me that we would be lucky to get $10,000 for a Nusiance Claim. I tried to get one Lawyer before the statues ran, but no luck. I heard that the Elder Abuse Statues ran for 7 years and to try for that. Oh well, I tried.

Joanie K.

I just started taking Vytorin and my doc told me if I had any muscle aches to call him. I haven't yet. But my symptoms are very tired all the time, my hamstrings and calves ache all the time as if I have the flu. I have an ache in my left arm, my joints ache like the flu, also my right him feels like its going to slip out of socket sometime when I stand and turn. My back hurts a lot as if I have bee lift weights with my back.My appetite is almost gone, that part I like however I go all day sometimes without being hungry or eating. Some mornings I wake up very, very thirsty. The worst symptoms is the body and joint aches. I was attempting to have sex with my wife everything started out fine then all of a sudden whammo, it turtled-up. I've experienced this before but only after playing 3 hours of basketball or weight lifting. I've only taken Vytorin every other day.

Took levaquin,500mg,for 10 days to combat infection in my left toe. Infection stopped,however pain in both calves is severe. Started on left leg then also rt. leg. Been off the med for 3 days. Seems to be better in am but gets awful as the day wears on. When will it stop? Is there long trm damage?

I have been taking Lisinopril 10mg every morning for about 1 1/2 months. I have been developing many different side effects, but primarily they consist of muscle cramps (painful!) in the legs/calves, numbness of feet with pain when walking, severe itching (it feels almost like ants walking all over my body), and horrible belching and flatulence. I did not connect it to the Lisinopril until I had ruled out all the other medications I have been taking and then coming across a web site that outlined the symptoms I have been experiencing. Why the symptoms occurred gradually and not all at the same time is bewildering, but it is definitely an allergic reaction of some type. I have discontinued the medication as of today and will call my Dr. in the morning and discuss (Yeah, like he'll really come to the phone!) The constellation of symptoms only highlights the strong and potentially life-threatening symptoms that could have occurred. A major anaphylactic reaction could have led to difficulty breathing, atrial fibrillation and probably death. The doctors who prescribe medications are not always aware of the potential harm that could result from the side effects of the meds they prescribe. It is vitally important that we report all symptoms to our doctors and/or pharmacists, nurses, etc. This drug may need to be further investigated. (An FDA approved drug which results in severe side effects can be pulled from the market and doctors told not to prescribe it while a further investigation is completed. Reading the previous posts, it is apparent that many individuals are having similar problems.
The itching is the WORST!!
My advice to anyone having even the slightest symptoms or if you are experiencing more severe reactions to report this to anyone who will listen. If your individual MD finds nothing wrong, invite him/her to imagine how devastating the symptoms can be and literally demand discontinuation of the drug and a prescription for a safer, effective drug.
The advertising campaigns for the drug companies constitute a very massive push to prescribe any and/or all of the meds brought to the marketplace with little regard for those of us who are suffering. This must not be allowed to continue. The unfortunate aspect of discontinuing this med is that the high blood pressure I currently have was fairly controlled by the Lisinopril, but the side effects are impossible and either a new med will be prescribed by my doctor (if he won't listen and/or try to understand, it is time to find a more enlightened physician!) Our fates rest on the combined efforts of all of us to bring the dangers of this med to the forefront. Our hypertension may not be controlled for a few days (until a doctor can prescribe a new one), but the alternative of continuing the med and ignoring or making light of the side effects is far worse.!

I am a 34 y/o male who started taking 10mg/day of lisinopril on May 15th. My blood pressure at the time was 140/118, pretty high I guess! I was feeling it too in the form of headaches. The doc wrote the script for me and I filled it that night. I should also mention that this is not the first time I have taken Lisinopril. I stopped taking it back in March because the script ran out. I don't seem to recall any kind of side-effects the first time, but I could be wrong. Anyway, I also take Levoxyl for my hypothyroidism, and it is a pretty hefty dose, 225mcg a day.

So, for the first week, I was doing pretty good on it. No coughing, or any of the listed side effects listed for the med. Then, about a week into it, I started having numbness in the right three toes on my right foot. When I say numb, I don't mean I could not feel anything, it was like touching your skin with a t-shirt over it. I could feel it, just kind of topically numb. I had a 'patch' of this numb skin right behind those same three toes and several other areas up the front and back of my right calve. I delt with this for a few days, thinking it was my shoes I was wearing at work. They were pretty worn out on the outer edges. I got new shoes on Monday, June 2nd. I wore them to work on the next day. At the end of the day, my calves felt kind of tired. The next day, they felt kind of tired still. I found this sort of weird. From that point on, my high anxiety really kicked in. I don't want to mention the thoughts I am having about what it could be that is causing this. I forgot to mention that I have not been sleeping well lately either since I started taking the Lisinppril again. I guess overall, I feel exhausted and weak. More so in my legs. To add to it, my lower back hurts like mad. I have two herniated discs and mild arthritis in it from damage from years ago. Also, for the past week, a pain has been developing in my left shoulder blade in my back. It is worse in the morning, and had gradually been getting worse for about a week. Today, it was awful.

I have ready a lot of the messages about the side effects different people are having. My question is, has anyone ever been on the lisinopril, gone off of it for whatever reason, having had no bad side effects, then gone back on it only to start having these bad side effects that you did not have before?

I have stopped taking the lisinopril on the 5th and have a doctor's appointment on the 9th to find out what is going on. I don't feel good at all. Can anyone relate?